- Chapter 1: Chemistry: An Introduction
- Chapter 10: Energy
- Chapter 11: Modern Atomic Theory
- Chapter 12: Chemical Bonding
- Chapter 13: Gases
- Chapter 14: Liquids and Solids
- Chapter 15: Solutions
- Chapter 16: Acids and Bases
- Chapter 17: Equilibrium
- Chapter 18: OxidationReduction Reactions and Electrochemistry
- Chapter 19: Radioactivity and Nuclear Energy
- Chapter 2: Matter
- Chapter 20: Organic Chemistry
- Chapter 21: Biochemistry
- Chapter 3: Chemical Foundations: Elements, Atoms, and Ions
- Chapter 4: Nomenclature
- Chapter 5: Measurements and Calculations
- Chapter 6: Chemical Composition
- Chapter 7: Chemical Reactions: An Introduction
- Chapter 8: Reactions in Aqueous Solutions
- Chapter 9: Chemical Quantities
World Of Chemistry 2nd Edition - Solutions by Chapter
Full solutions for World Of Chemistry | 2nd Edition
An unsaturated hydrocarbon that contains one or more carbon-carbon triple bonds.
The increase in energy associated with a bond angle that has deviated from the preferred angle of 109.5°.
An acid that is not a proton donor; an acid that is an electron pair acceptor in a Lewis acid-base reaction.
A reaction in which two species are involved in the rate-determining step.
A substance composed of atoms of two or more elements chemically united in fixed proportions. (1.4)
Structural isomers of coordination compounds in which the ligands within the coordination sphere differ. (Section 23.4)
Electrons that are spread over a number of atoms in a molecule or a crystal rather than localized on a single atom or a pair of atoms. (Section 9.6)
Refers to the steric strain arising from interaction between an axial substituent and an axial hydrogen (or other group) on the same side of a chair conformation of a cyclohexane ring
A procedure for preparing a less concentrated solution from a more concentrated solution. (4.5)
Carbohydrates comprisedof two monosaccharide units joined via aglycosidic linkage between the anomeric carbonof one monosaccharide and a hydroxyl group ofthe other monosaccharide.
For alkenes, a stereodescriptorthat indicates that the two priority groups are on opposite sides of the p bond.
A carbanion with the structure RMgX.
A representation of covalent bonding in a molecule that is drawn using Lewis symbols. Shared electron pairs are shown as lines, and unshared electron pairs are shown as pairs of dots. Only the valence-shell electrons are shown. (Section 8.3)
The term used to describe the wave characteristics of a moving particle. (Section 6.4)
Theresonance-stabilized intermediate of a nucleophilicaromatic substitution reaction.
The study of carbon-containing compounds, typically containing carbon–carbon bonds. (Section 2.9; Chapter 24:Introduction)
Changes (such as a phase change) that occur with no change in chemical composition. (Section 1.3)
A series of intermediates and curved arrows that show howthe reaction occurs in terms of the motion of electrons.
For mechanisms, a step that involves three chemical entities.
A solution prepared by dissolving Ag2O in aqueous ammonia; used for selective oxidation of an aldehyde to a carboxylic acid.
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